Less Ads, More Data, More Tools Register for FREE

Pin to quick picksFaron Pharmaceuticals Regulatory News (FARN)

Share Price Information for Faron Pharmaceuticals (FARN)

Share Price is delayed by 15 minutes
Get Live Data
43.50    0.00 (0.00%)
Bid:
42.00
Ask:
45.00
Spread: 3.00 (7.143%)
Market Cap: £88.25m
FARN Live PriceLast checked at - London Stock Exchange

Intraday Faron Pharmaceuticals Share Chart

Phase II INFORAAA study update

26 Jun 2019 07:00

RNS Number : 4090D
Faron Pharmaceuticals Oy
26 June 2019
 

Faron Pharmaceuticals Oy

("Faron" or the "Company")

 

Phase II INFORAAA study update

Interim analysis supports continuation of study

 

TURKU - FINLAND, 26 June 2019 - Faron Pharmaceuticals Oy (AIM: FARN), the clinical stage biopharmaceutical company, today announces interim results from the Phase II INFORAAA study, which examined the effect of Traumakine on mortality (predominantly for Multi-Organ Failure, MOF) and pharmacodynamic biomarkers of surgically operated Ruptured Abdominal Aorta Aneurysm (RAAA) patients.

 

Traumakine treatment during the INFORAAA trial was identical to the INTEREST trial with treatment once a day for six days following surgical operation. The ratio of the treatment arm versus placebo was two to one and mortality was assessed for a period of 30 days after surgery. RAAA patients suffer two cycles of a potential ischemic injury to the vascular endothelium: the first caused by the rupture of the aorta and the resulting hemodynamic and circulatory collapse, which is then followed by the cross-clamping and un-clamping of the aorta leading to reperfusion injury. These mechanisms contribute to hypoxia-induced inflammation and multi organ failure, which is the main cause of death within the first 5-10 days. The expected mortality is normally between 30-50% of all operated patients.

 

A total of 35 patients were included in the interim read out, 25 of which were treated with Traumakine and 10 of which received placebo. Biomarker (MxA and CD73) responses indicated a good interferon response. Unexpectedly, concomitant corticosterone was recorded both in the active (28%) and placebo (30%) treatment arm. Measurement of CD73 serum concentrations indicated that this concomitant corticosteroid use abolished a CD73 response, as observed earlier in all three previous studies (two independent phase III and the YODA study). Patients without Traumakine-induced CD73 values were more likely to die than those with induction. Unfortunately, while the removal of corticosteroid-treated patients from statistical analysis reduced group sizes and made statistical mortality analysis meaningless, a trend toward reduction of mortality was seen in the Traumakine-treated patients who did not receive corticosteroids. Mortality in various groups varied from 15-20%, except in those patients without induced CD73 concentrations - mortality in that group was high with 6 out of 7 (85.7%) not surviving.

 

Based on the study's predefined decision criteria and statistical analysis of mortality in the active and placebo treatment arms the study may proceed. The Company will evaluate these data, together with previously announced data from the YODA trial and post-hoc INTEREST data to finalise its plans for future Traumakine development and will make further announcements in due course.

 

Dr Markku Jalkanen, Chief Executive Officer of Faron, said: "The INFORAAA interim data is very important to us as it again shows the protective effects of CD73 activation without the presence of steroids. It is still too early to estimate the efficacy of Traumakine in this setting because of the limited number of evaluable patients without concomitant steroids, however the interim analysis supports the continuation of the study according to current powering. It was disappointing to learn about this magnitude of steroid use in this patient population as RAAA is considered as a traumatic condition and to have only limited inflammatory impact on disease development."

 

This announcement contains inside information for the purposes of Article 7 of Regulation (EU) No 596/2014 ("MAR").

 

 

For more information please contact:

 

Faron Pharmaceuticals Oy

Dr Markku Jalkanen, Chief Executive Officer

investor.relations@faron.com 

 

Panmure Gordon (UK) Limited, Nomad and Broker

Emma Earl, Freddy Crossley (Corporate Finance)

James Stearns (Corporate Broking)

Phone: +44 207 886 2500

 

Consilium Strategic Communications

Mary-Jane Elliott, David Daley, Lindsey Neville

Phone: +44 (0)20 3709 5700

E-mail: faron@consilium-comms.com

 

Westwicke Partners, IR (US)

Chris Brinzey

Phone: 01 339 970 2843

E-Mail: chris.brinzey@westwicke.com

 

About Ruptured Abdominal Aortic Aneurysm (RAAA)

Ruptured Abdominal Aortic Aneurysm (RAAA) is a surgical emergency with an overall mortality of 70 to 80%. It requires immediate surgery and aortic repair. Approximately half of the deaths of RAAA patients is due to not reaching the hospital in time, and despite immediate surgery and intensive care treatment, the second half dies in hospital within 30 days post-operatively, mostly due to multi-organ failure. The cause of high post-operative mortality is mainly due to prolonged hypotension/hypoxia from the ruptured aorta and the aftermath of restoring blood flow: reperfusion, vascular leakage and failure of vital organs. Currently there are an estimated 40,000 US and European patients per annum eligible for the treatment, making this an orphan indication.

 

About Faron Pharmaceuticals Ltd

Faron (AIM:FARN) is a clinical stage biopharmaceutical company developing novel treatments for medical conditions with significant unmet needs. The Company currently has a pipeline focusing on acute organ traumas, vascular damage and cancer immunotherapy. The Company's first candidate Traumakine, to prevent vascular leakage and organ failures, has completed a Phase III clinical trial in Acute Respiratory Distress Syndrome (ARDS). An additional European Phase II Traumakine trial is underway for the Rupture of Abdominal Aorta Aneurysm ("RAAA"). Faron's second candidate Clevegen is a ground breaking early clinical anti-Clever-1 antibody. Clevegen has the ability to switch immune suppression to immune activation in various conditions, with potential across oncology, infectious disease and vaccine development. This novel macrophage-directed immuno-oncology switch called Turn-on-your-Immunity or Turn-It may be used alone or in combination with other immune checkpoint molecules for the treatment of cancer patients. Faron is based in Turku, Finland. Further information is available at www.faron.com

 

 

This information is provided by RNS, the news service of the London Stock Exchange. RNS is approved by the Financial Conduct Authority to act as a Primary Information Provider in the United Kingdom. Terms and conditions relating to the use and distribution of this information may apply. For further information, please contact rns@lseg.com or visit www.rns.com.
 
END
 
 
RESBRGDLRBDBGCU
Date   Source Headline
9th Feb 20265:35 pmMFNInside Information: Faron Pharmaceuticals Ltd is planning a rights offering of approximately EUR 40 million to strengthen its capital structure and to drive lead asset bexmarilimab to key milestones
3rd Feb 20264:00 pmMFNFaron Pharmaceuticals Ltd: Registration of New Shares
3rd Feb 20267:00 amMFNFaron Pharmaceuticals Ltd: Approval of Share Subscriptions Based on Special Rights in connection with Amortisation of the First and Second Tranche Bonds
13th Jan 20264:00 pmMFNFaron Pharmaceuticals Ltd: PDMR Dealing
8th Jan 20265:45 pmMFNFaron Pharmaceuticals Ltd: Approval of Share Subscriptions Based on Special Rights in connection with Advanced Amortisation of the First Tranche Bonds
17th Dec 20252:30 pmMFNComposition of Faron Pharmaceutical's Shareholders' Nomination Board
11th Dec 20258:30 amMFNFaron issues second tranche of bonds with an aggregated principal amount of EUR 10 million under its convertible bond arrangement
4th Dec 20254:00 pmMFNFaron Pharmaceuticals Ltd: Holding(s) in Company
3rd Dec 202510:00 amMFNFaron Pharmaceuticals Ltd: Registration of New Shares
3rd Dec 20257:00 amMFNFaron Pharmaceuticals Ltd: Approval of Share Subscriptions Based on Special Rights in connection with Amortisation of the First Tranche Bonds
2nd Dec 20257:00 amMFNFaron Pharmaceuticals Ltd: Grant of Options
1st Dec 20257:00 amMFNFaron Pharmaceuticals Ltd: Appointment of CFO
27th Nov 20257:00 amMFNFaron's Financial Calendar for 2026
20th Oct 20256:00 amMFNUpdated BEXMAB Phase I/II Data presented at ESMO 2025 shows further improvement, strengthening the clinical profile of bexmarilimab in treatment-naïve HR-MDS patients
3rd Oct 202510:00 amMFNFaron Pharmaceuticals Ltd: Registration of New Shares
3rd Oct 20256:00 amMFNFaron Pharmaceuticals Ltd: Approval of Share Subscriptions Based on Special Rights in connection with Amortisation of the First Tranche Bonds
19th Sep 20256:00 amMFNFaron Pharmaceuticals Ltd: Exercise of Options, Director Dealing and Issue of Equity
12th Sep 20253:25 pmMFNCorrection: FARON PHARMACEUTICALS LTD: HALF-YEAR FINANCIAL RESULTS 1 JANUARY - 30 JUNE 2025
27th Aug 20256:00 amMFNFARON PHARMACEUTICALS LTD: HALF-YEAR FINANCIAL RESULTS 1 JANUARY - 30 JUNE 2025
19th Aug 20256:00 amMFNFaron Pharmaceuticals Ltd: Notice of Half-Year Financial Results
18th Aug 20256:00 amMFNInside Information: Faron to advance bexmarilimab into a registrational Phase 2/3 study in treatment-naïve (frontline) HR-MDS after positive meeting with the FDA
8th Aug 20252:00 pmMFNFaron Pharmaceuticals Ltd: Holding(s) in Company
7th Aug 20256:00 amMFNFaron Pharmaceuticals Ltd: Approval of Share Subscriptions Based on Special Rights in connection with Advanced Amortisation of the First Tranche Bonds
6th Aug 20256:00 amMFNInside Information: Faron to present updated BEXMAB data in frontline HR-MDS to FDA; complete remission rate substantially increased to 43%
2nd Jul 202510:00 amMFNFaron Pharmaceuticals Ltd: Director Dealing
30th Jun 202511:00 amMFNFaron Pharmaceuticals Ltd: Director/PCA Dealing
5th Jun 20253:00 pmMFNFaron Pharmaceuticals Ltd: Director/PCA Dealing and Donation of Shares to Foundation
3rd Jun 202511:00 amMFNFaron Pharmaceuticals Ltd: Registration of New Shares
3rd Jun 20256:00 amMFNFaron Pharmaceuticals Ltd: Approval of Share Subscriptions Based on Special Rights in connection with Amortisation of the First Tranche Bonds
27th May 20254:00 pmMFNFaron Pharmaceuticals Ltd: Issue of Treasury Shares to the Company
21st May 20256:00 amMFNFaron Appoints Ralph Hughes as Chief Business Officer (CBO)
14th May 20251:00 pmMFNFaron Pharmaceuticals Ltd: Grant of Options
17th Apr 202512:15 pmMFNHolding in Company
15th Apr 20256:00 amMFNInside Information: Faron Announces Positive Phase II results in higher-risk myelodysplastic syndrome
3rd Apr 20256:00 amMFNInside Information: Faron enters into an up to EUR 35 million convertible bond arrangement and issues first tranche of bonds with a principal amount of EUR 15 million
21st Mar 20251:15 pmMFNBoard Changes
21st Mar 202511:45 amMFNResults of the Annual General Meeting, Change of Directors, Decision of the Board meeting after the AGM
20th Mar 20257:00 amMFNShareholders' Nomination Board updates its recommendation on the number of Board members to be elected and the persons proposed to be elected
3rd Mar 202512:05 pmRNSFDA Grants Orphan Drug Designation
3rd Mar 202512:00 pmMFNInside Information: FDA Grants Orphan Drug Designation for Bexmarilimab in MDS
28th Feb 202512:00 pmMFNNOTICE OF FARON PHARMACEUTICALS LTD'S ANNUAL GENERAL MEETING
28th Feb 202512:00 pmRNSNotice of Annual General Meeting
27th Feb 20257:30 amMFNInside Information: Faron Receives Positive EMA Opinion on Orphan Drug Designation for Bexmarilimab for the treatment of myelodysplastic syndrome (MDS)
27th Feb 20257:30 amRNSPositive EMA Opinion on Orphan Drug Designation
27th Feb 20257:15 amRNSAnnual Report 2024 published
27th Feb 20257:15 amMFNFaron Pharmaceuticals Ltd's Annual Report 2024 published
27th Feb 20257:00 amRNSFinancial Statement 1 January to 31 December 2024
27th Feb 20257:00 amMFNFaron's Financial Statement Release 1 January to 31 December 2024
19th Feb 202510:00 amRNSNotice of Financial Statement and Annual Report
14th Feb 202512:00 pmMFNHolding(s) in Company

Due to London Stock Exchange licensing terms, we stipulate that you must be a private investor. We apologise for the inconvenience.

To access our Live RNS you must confirm you are a private investor by using the button below.